5-PLASMA Bivalirudin Control, Model Number 5D-44905
US5-PLASMA Bivalirudin Control, Model Number 5D-44905
Recalling Firm: Aniara Diagnostica LLC
Grund für den Rückruf / Gefahr
TranslatedStability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values.
Produktbeschreibung & Identifikation
Translated5-PLASMA Bivalirudin Control, Model Number 5D-44905
Additional Source Details
| Field | Value |
|---|---|
| City | West Chester |
| State | OH |
| Event id | 99344 |
| Address 1 | 7768 Service Center Dr |
| Code info | UDI-DI: 05070002420385, Lot Number: KE132602 |
| Postal code | 45069-2442 |
| Report date | 20260812 |
| Product type | Devices |
| Product quantity | 9 units |
| Reason for recall | Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260701 |
| Initial firm notification | Letter |
| Center classification date | 20260805 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought 5-PLASMA Bivalirudin Control, Model Number 5D-44905?
Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (FDA Devices). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Übersicht
- Rückrufendes UnternehmenAniara Diagnostica LLC
- StatusOngoing
- RisikostufeClass II
- DistributionUS Nationwide distribution in the states of IL, NC, TN.
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🚨 SAFETY ALERT: Aniara Diagnostica LLC - 5-PLASMA Bivalirudin Control, Model Number 5D-44905 Check if your household is affected: https://therecallfile.com/de/recalls/5-plasma-bivalirudin-control-model-number-5d-44905/FDA-Z-2896-2026
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